Our Team

Meet the experts behind our success

Leadership Message

At AQniX Research Solutions, we believe the future of clinical research lies in the synergy between scientific integrity and digital innovation. Our purpose is clear to remove inefficiencies, close regulatory gaps, and enable a smarter, connected, and compliant research ecosystem. Our leadership team combines expertise in clinical operations, regulatory strategy, data management, and quality systems, united by a shared goal: to deliver excellence without compromise. By creating a digital environment, we ensure every step of research is transparent, traceable, and globally compliant. Every project we deliver reflects our commitment to lead with quality, think with innovation, and execute with integrity. We’re not just advancing clinical research. We’re redefining how research is done.

Dhara Podiya

MS. DHARA PODIYA

Co-Founder at AQniX Research Solutions

Clinical Quality & Compliance Strategist | Risk-Based Monitoring | 11+ Yrs in BA/BE Trial Execution | International (USFDA, EMA, WHO, ANVISA, TGA, DCGI) Inspection Readiness Specialist | Led 150+ BA/BE & Phase I–III Trials | CTMS Implementation Expert

As Co-founder of AQniX Research Solutions, she plays a pivotal role in driving the company’s strategic and technical direction. She has led the integration of AI-based CTMS platforms, established quality-centric workflows, and helped forge global partnerships aimed at expanding AQniX service capabilities. Her leadership style is innovation-driven, process-focused, and deeply rooted in compliance, helping position AQniX as a trusted partner in clinical research. With a focus on efficiency, transparency, and data-driven decision-making and continues to champion the company’s mission of delivering excellence in clinical innovation.

PROFESSIONAL EXPERIENCE:
Throughout her illustrious career, she has held pivotal leadership positions at some of the most respected institutions in clinical research, including Radiance Hospital, Veeda Lifesciences, and Synchron Research. In each of these esteemed organizations, she has demonstrated exceptional acumen in operational leadership, strategic execution, and the development of robust quality systems. Renowned for her unwavering commitment to excellence, she has played a transformative role in the successful execution of complex clinical trials particularly in the critical therapeutic area of Neurology, Oncology, psychiatry, gastrointestinal, ophthalmology, dermatology and Immunosuppressant ensuring full alignment with stringent global regulatory standards. Her expertise extends far beyond trial management; she has consistently pioneered operational frameworks that elevate compliance, drive innovation, and set new benchmarks for quality in clinical research.

With a proven track record of delivering impactful outcomes in highly regulated and high-stakes environments, she continues to be a force of vision and precision, seamlessly integrating scientific integrity with operational excellence at every stage of clinical development.

SPECIALIZED EXPERTISE:
She core strengths lie in Quality Management Systems (QMS), clinical data integrity, data management, and process optimization. She has demonstrated expertise in using clinical technologies such as CTMS, eCRF, DMS, PheeDIt, and Clinion, and has developed tools and processes that streamline data capture and reporting. A key innovation she led was the design of a proprietary risk-based monitoring system, aimed at improving efficiency and quality in clinical oversight. Her approach to documentation, SOP compliance, and system integration reflects her commitment to operational excellence and audit-readiness.

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